We narrowed to 994 results for: Ran
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TypeBlog Post...concentration of any experimental wells in that range of optical densities. If your standard curve does...
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A Guide to Designing a Scientific Poster: Content, Layout, and More
TypeBlog Post...inserted into larger circles or ovals, that are arranged in some logical pattern across the poster. This... -
Meet an Addgenie: Insights into Grad School, Career Paths, and More
TypeBlog Post...Development, got her PhD in Plant Biochemistry in France. When she moved to the U.S., she discovered that... -
Tips for Technical Support Calls
TypeBlog Post...probably difficult for you to ascertain where on this range your question falls. Here are some things to keep... -
High Complexity Golden Gate Assembly with NEB’s DAD
TypeBlog Post...up to 10-12 fragments (Pryor et al., 2020), and randomly selected non-palindromic pairs allows for high-fidelity... -
A Look at Addgene's QC Process
TypeBlog Post...accuracy across all of our plasmids and provide transparency in sequence discrepancies. While Addgene’s QC... -
Lentivirus ddPCR Titration
TypeProtocol... is based on an LV titer range of 1E+05–1E+09 TU/mL, where TU is transducing units and generally represents...July 7, 2023 Workflow Timeline Day 1: Seed and transduce cells Day 4: Treat cells with Benzonase and harvest...Complete 3 µL of 250 U/µL benzonase Procedure Transducing Cells Thaw the virus on ice. Prepare the following... pipette 10–20 times. Use a new pipette tip to transfer 200 µL of the first dilution into the next dilution... plate (1 dilution per well). Leave one well untransduced (add 150 µL of DMEM complete instead of a viral... into the wells containing the virus and the untransduced control. Pro-Tip For even seeding, prepare a...min. Resuspend cells in 500 µL DMEM complete and transfer to a microcentrifuge tube. Centrifuge for 5 min... -
The Scientific Conference Poster Session: Tips for Success
TypeBlog Post...how best to prepare. Maybe you’re a presentation veteran, but have difficulty answering questions. Or perhaps... -
Tips to Make the Most of a Scientific Conference
TypeBlog Post...overwhelming when you are presented with a sea of strangers. Try things like sitting at a table for lunch ... -
Experimenting with New Careers while in Grad School
TypeBlog Post...speakers each week, my department and graduate office arranged opportunities to meet with various professionals... -
Antibodies 101: Conventional vs Spectral Flow Cytometry
TypeBlog Post...the markers in the panel. This complexity index ranges from 0-1, with a value of “0” indicating those ... -
Of Myc and Men
TypeBlog Post...an amide group added to its C-terminus post-translationally, which turned out to be critical for antibody... -
PhD Applications After COVID
TypeBlog Post...lab, research, and provide them with a CV or transcripts if requested Thank them, and eagerly await a ... -
Sharing Your Lab Protocols: Using Apps to Save Time & Track Your Experiments
TypeBlog Post...restriction digest of plasmid DNA, and bacterial transformation. And more plasmid-related educational resources... -
What is Polymerase Chain Reaction (PCR)
TypeProtocol...step heats the double stranded DNA template strand to the point where the strands start denaturing and ...this temperature range to anneal to each of the single stranded DNA template strands. The DNA polymerase...of the sense and anti-sense strands of the template DNA. They are strands of nucleic acid that are starting...molar ratio. It also requires two unique single stranded DNA oligonucleotide (oligo) primers, which anneal...seconds at 94°C: Continued denaturation of double stranded DNA. Anneal primers for 30 seconds at 55°C: The...polymerase to synthesize and elongate the new target DNA strand accurately and rapidly. Repeat steps 2-4 25-30 ...fill-in any protruding ends of the newly synthesized strands. Materials List Reagents for each 50µL PCR: Thin-walled... -
CRISPR Library Amplification
TypeProtocol... Day 1: Transform, recover, set up overnight growth (Estimated time 2-3 hours) Transformation should be...of 5 mL (3 mL SOC + 2 mL transformed Endura from two separate transformations). Pro-Tip Do not pipette...assumes familiarity with standard bacterial transformation and basic knowledge of the library being amplified...amplified. Please see our protocol on Bacterial Transformation . The generalized pooled library amplification...premixed LB (VWR 101414-072) for convenience but any brand or house- made LB that supports normal growth is...using a new vented falcon tube for every two transformations. Each of the four 14 mL Vented Falcon Tubes...repeatedly or mix when removing SOC containing transformed DNA-Endura from cuvette. Shake four 14 mL Vented... -
Protocol - Over-Agar Antibiotic Plating
TypeProtocol...incubation, transform DH5α E. coli cells by heatshock with the plasmid of interest. See our transformation page...for a detailed heatshock transformation protocol. Plate 50 µL of transformed E. coli /rescue media suspension...also like... Making LB Agar Plates Bacterial Transformation Recovering Plasmid DNA from Bacterial Culture...plating antibiotic over-agar for the selection of transformed E. coli . Over-agar spreading of antibiotic makes...investigator to conveniently plate and select transformed cells containing plasmids differing in their ... sterile water (or other antibiotic) E. coli transformed with a plasmid containing the carbenicillin (...carbenicillin, plated over-agar for selection of transformed E. coli . Sample Data Selection of E.coli on ... -
A Guide to Starting Your Own Journal Club
TypeBlog Post...of current new and exciting literature. As I transitioned out of academia and away from the bench I certainly... -
Controlling for Off-target Effects with a New Genome-wide CRISPR Screen Design
TypeBlog Post...DNase hypersensitivity, or are in an enhancer, transcription factor binding site, or a coding region. Targeting... -
Neuronal labeling with Spaghetti Monster
TypeBlog Post...ideal probe should combine the solubility, cell tolerance, and optional fluorescence of FPs with facile ...